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Comprehensive characterization of myeloid cells during wound healing in healthy and healing‐impaired diabetic mice
Wound healing involves the concerted action of various lymphoid and in particular myeloid cell populations. To characterize and quantitate different types of myeloid cells and to obtain information on their kinetics during wound healing, we performed multiparametric flow cytometry analysis. In healt...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496577/ https://www.ncbi.nlm.nih.gov/pubmed/32306381 http://dx.doi.org/10.1002/eji.201948438 |
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author | Joshi, Natasha Pohlmeier, Lea Ben‐Yehuda Greenwald, Maya Haertel, Eric Hiebert, Paul Kopf, Manfred Werner, Sabine |
author_facet | Joshi, Natasha Pohlmeier, Lea Ben‐Yehuda Greenwald, Maya Haertel, Eric Hiebert, Paul Kopf, Manfred Werner, Sabine |
author_sort | Joshi, Natasha |
collection | PubMed |
description | Wound healing involves the concerted action of various lymphoid and in particular myeloid cell populations. To characterize and quantitate different types of myeloid cells and to obtain information on their kinetics during wound healing, we performed multiparametric flow cytometry analysis. In healthy mice, neutrophil numbers increased early after injury and returned to near basal levels after completion of healing. Macrophages, monocyte‐derived dendritic cells (DCs), and eosinophils were abundant throughout the healing phase, in particular in early wounds, and Langerhans cells increased after wounding and remained elevated after epithelial closure. Major differences in healing‐impaired diabetic mice were a much higher percentage of immune cells in late wounds, mainly as a result of neutrophil, macrophage, and monocyte persistence; reduced numbers and percentages of macrophages and monocyte‐derived DCs in early wounds; and of Langerhans cells, conventional DCs, and eosinophils throughout the healing process. Finally, unbiased cluster analysis (PhenoGraph) identified a large number of different clusters of myeloid cells in skin wounds. These results provide insight into myeloid cell diversity and dynamics during wound repair and highlight the abnormal inflammatory response associated with impaired healing. |
format | Online Article Text |
id | pubmed-7496577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74965772020-09-25 Comprehensive characterization of myeloid cells during wound healing in healthy and healing‐impaired diabetic mice Joshi, Natasha Pohlmeier, Lea Ben‐Yehuda Greenwald, Maya Haertel, Eric Hiebert, Paul Kopf, Manfred Werner, Sabine Eur J Immunol Tissue immunology and leukocyte trafficking Wound healing involves the concerted action of various lymphoid and in particular myeloid cell populations. To characterize and quantitate different types of myeloid cells and to obtain information on their kinetics during wound healing, we performed multiparametric flow cytometry analysis. In healthy mice, neutrophil numbers increased early after injury and returned to near basal levels after completion of healing. Macrophages, monocyte‐derived dendritic cells (DCs), and eosinophils were abundant throughout the healing phase, in particular in early wounds, and Langerhans cells increased after wounding and remained elevated after epithelial closure. Major differences in healing‐impaired diabetic mice were a much higher percentage of immune cells in late wounds, mainly as a result of neutrophil, macrophage, and monocyte persistence; reduced numbers and percentages of macrophages and monocyte‐derived DCs in early wounds; and of Langerhans cells, conventional DCs, and eosinophils throughout the healing process. Finally, unbiased cluster analysis (PhenoGraph) identified a large number of different clusters of myeloid cells in skin wounds. These results provide insight into myeloid cell diversity and dynamics during wound repair and highlight the abnormal inflammatory response associated with impaired healing. John Wiley and Sons Inc. 2020-05-13 2020-09 /pmc/articles/PMC7496577/ /pubmed/32306381 http://dx.doi.org/10.1002/eji.201948438 Text en © 2020 The Authors. European Journal of Immunology published by Wiley‐VCH Verlag GmbH & Co. KGaA This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Tissue immunology and leukocyte trafficking Joshi, Natasha Pohlmeier, Lea Ben‐Yehuda Greenwald, Maya Haertel, Eric Hiebert, Paul Kopf, Manfred Werner, Sabine Comprehensive characterization of myeloid cells during wound healing in healthy and healing‐impaired diabetic mice |
title | Comprehensive characterization of myeloid cells during wound healing in healthy and healing‐impaired diabetic mice |
title_full | Comprehensive characterization of myeloid cells during wound healing in healthy and healing‐impaired diabetic mice |
title_fullStr | Comprehensive characterization of myeloid cells during wound healing in healthy and healing‐impaired diabetic mice |
title_full_unstemmed | Comprehensive characterization of myeloid cells during wound healing in healthy and healing‐impaired diabetic mice |
title_short | Comprehensive characterization of myeloid cells during wound healing in healthy and healing‐impaired diabetic mice |
title_sort | comprehensive characterization of myeloid cells during wound healing in healthy and healing‐impaired diabetic mice |
topic | Tissue immunology and leukocyte trafficking |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496577/ https://www.ncbi.nlm.nih.gov/pubmed/32306381 http://dx.doi.org/10.1002/eji.201948438 |
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